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Chat mode
Conversational mode
Curtain mode
Curtained mode
European market opportunities for modes of transport
H mode
Interaction mode
Interactive mode
Markets for different modes of transportation
Markets for modes of transport
Markets for modes of transportation
Master mode
Mode changer
Mode converter
Mode convertor
Mode of interaction
Mode transformer
Monitor mode
Pillar box mode
Pillar-box mode
Pillarbox mode
Privileged mode
SL mode
Side bar mode
Side-bar mode
Sidebar mode
Sidebarred mode
Single-line mode
Supervisor mode
TE mode
Talk mode
Time sharing mode
Transverse electric mode

Traduction de «sl mode » (Anglais → Français) :



A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL

myopathie métabolique par défaut de transport du lactate


mode changer | mode converter | mode convertor | mode transformer

convertisseur de mode | transformateur de mode


pillarbox mode [ pillar-box mode | pillar box mode | curtained mode | curtain mode | sidebarred mode | side-bar mode | side bar mode | sidebar mode ]

mode colonne


master mode | monitor mode | privileged mode | supervisor mode

mode maître | mode superviseur


European market opportunities for modes of transport | markets for different modes of transportation | markets for modes of transport | markets for modes of transportation

marchés des modes de transport


interactive mode [ chat mode | conversational mode | interaction mode | mode of interaction | talk mode | time sharing mode ]

mode interactif [ mode dialogué | mode conversationnel | téléconversation | mode de bavardage ]


H mode | TE mode | transverse electric mode

mode électrique | mode électrique transverse | mode H | mode TE


This syndrome has characteristics of severe intellectual deficit, brachycephaly, plagiocephaly, prominent forehead and coarse facial features. It has been described in two males from one family. Two females belonging to the same family displayed mode

syndrome de déficience intellectuelle liée à l'X-plagiocéphalie


Syndrome with the association of diffuse palmoplantar keratoderma and acrocyanosis. It has been described in eight members of one family and in two sporadic cases. The mode of inheritance in the familial cases was autosomal dominant.

syndrome de kératodermie palmoplantaire diffuse-acrocyanose




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Date index: 2021-04-06
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